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Our Peers - Empowerment and Navigational Support - Community Living (OP-ENS-CL): A Peer Navigator Intervention for Adults With Acquired Physical Disabilities

Our Peers - Empowerment and Navigational Support - Community Living (OP-ENS - CL)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06941233
Acronym
OP-ENS-CL
Enrollment
100
Registered
2025-04-23
Start date
2025-12-01
Completion date
2027-08-01
Last updated
2026-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Disabled Persons

Keywords

peer navigators, community health worker

Brief summary

The goal of this clinical trial is to learn if a remote peer navigator intervention (OP-ENS - CL) for people with newly acquired physical disabilities returning to community living after rehabilitation improves self-reported social support, health, and community participation. The main questions it aims to answer are: Do people with acquired physical disabilities who receive the remote peer navigator intervention experience greater social support and self-efficacy than people in the control group? Do people with acquired physical disabilities who receive the remote peer navigator intervention have better self-reported health and social participation outcomes than people in the control group? Is the OP-ENS - CL intervention acceptable to people with newly acquired physical disabilities returning to community living?

Detailed description

The purpose of this study is to evaluate the efficacy and social validity of the OP-ENS - CL (Our Peers - Empowerment and Navigational Support - Community Living) a remote 12-month peer navigator intervention using a clinical trial design in a sample of adults with newly acquired with physical disabilities transitioning to community living. Participants will be recruited through community and clinical networks and screened for eligibility. Participants will be randomly assigned to either the intervention or usual care groups. Participants in the intervention group will be matched with a trained peer health navigator (who is also a person with a physical disability). Using a structure process of barrier identification, goal setting and action planning peer health navigators will work with participants to help address their healthcare needs and concerns, including such things as patient-provider communication, transportation, access to durable medical equipment. It is important to note that peer health navigators are not healthcare providers and do not provide medical or health advice. Participants in the intervention trial are asked to meet with their peer navigator at least once a month during the study period. To encourage participation in this intervention, progressive micro-incentives are integrated into the study protocol. To promote equipoise, a similar micro-incentive schedule is created for the usual care group. Data Collection - All participants, regardless of group assignment, will be interviewed at 3 time points (baseline, 6 months, 13 months) using a self-report measures of healthcare access, quality, and outcomes as well as measures of social support and patient activation. Data collectors will be blinded to group assignment and not involved in the delivery of the OP-ENS - CL intervention. Data Analysis - The investigators will employ mixed effects model using each study outcome as a time-varying dependent variable and treatment group (PHN vs. usual care) as the main fixed effect. Baseline characteristics including race/ethnicity, gender, and socioeconomic status will be entered as time-invariant covariates if baseline group differences are observed (in spite of randomization). Subject intercept will be modeled as a random effect. The null hypothesis will be rejected if a significant group\*time interaction effect is observed. The investigators hypothesize that PN will have a more favorable trajectory slope of study outcomes than the matched control group. For each hypothesis, post-hoc analysis will be conducted to assess difference in each outcome variable between the two groups at different time points. The mixed models will run using PROC MIXED from of SAS 9.3 (Cary, NC). The method of estimation will be maximum likelihood (ML). A variety of covariance structures (first order regressive, compound symmetry, toeplitz, variance components, unstructured) will be carefully examined and compared for best model fit, Akaike's Information (AIC) and Bayesian Information Criteria (BIC). These statistics are functions of the log likelihood and can be compared across models. As missing data are inevitable in a longitudinal study, values will be imputed where possible using either mean (median) substitute or formal imputation procedures such as EM algorithm if missing data are MCAR (missing completely at random) or MAR (missing at random). If missing data are NMAR (not missing at random), the "pattern mixture" approach will be used to compute a "weighted average" of the parameters that are associated with the missing data to estimate what the data would have been.

Interventions

BEHAVIORALOur Peers - Empowerment and Navigational Support - Community Living (OP-ENS - CL)

Op-ENS - CL is a 12-month, remote delivered peer navigator intervention. Participants will meet with a trained peer navigator who mentors nad supports them through a manualized process of collaborative conversations, barrier identification, asset mapping, goal setting, and action planning along with on-going social support and information sharing.

Sponsors

Susan Magasi
Lead SponsorOTHER
Northwestern University
CollaboratorOTHER
Shirley Ryan AbilityLab
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

Given the nature of the intervention it is not possible to mask participants and interventionists to group assignment. Outcome assessor and investigators will be unaware of group assignment.

Intervention model description

Participants will be randomly assigned to either the intervention or usual care groups using block randomization with randomly selected blocks of 4, 8, or 12. Randomization sequence will be generated using SAS algorithm.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1) Self-identify as a person with physical disability due to a neurological condition, including SCI, stroke, TBI, multiple sclerosis, or Parkinson's disease (according to the American Community Survey 6-Items), 2) onset of disability within the last 6 months, 3) transitioned to community living in the past 4 months, 4) able to speak, read and understand English, 5) own or have regular access to either a smartphone (Android or iOS operating system), tablet, laptop, or desktop computer with internet access. 6) adults 18 years of age or older, 7) able to provide informed consent.

Exclusion criteria

1) Cognitive, sensory, or physical functional limitations that interfere with effective use of the OP-ENS - CL app.

Design outcomes

Primary

MeasureTime frameDescription
Patient Activation MeasureBaseline, 6 months, 13 months.The 13-item self-report measure assesses perceived knowledge, skills, and confidence for self-management
PROMIS Self-Efficacy Short FormBaseline, 6 months, 13 months.4-item self-report short form measure assessing confidence in one's ability to perform specific tasks or behaviors
PROMIS Emotional Support, short formBaseline, 6 months, 13 months.8-item self-report short forms assessing the availability of 3 types of emotional support
PROMIS informational support, short formBaseline, 6 months, 13 months.8-item self-report short forms assessing the availability of informational support
PROMIS Instrumental Support, short formBaseline, 6 months, 13 months.8-item self-report short forms assessing the availability of instrumental support

Secondary

MeasureTime frameDescription
PROMIS Global HealthBaseline, 6 months, 13 months.8-item self-report short form assessing perceived physical, mental, and social health.
PROMIS DepressionBaseline, 6 months, 13 months.8-item short form assessing self-reported affect, views of self, social cognition, and decreased positive affect
PROMIS Ability to Participate in Social Roles and ActivitiesBaseline, 6 months, 13 months.8-item short form assessing perceived ability to perform one's usual social roles and activities
Community Participation Indicators, Enfranchisement ScaleBaseline, 6 months, 13 months.19-item self-report measures 3 subjective domains of participation, choice and control, contributing to one's community, and feeling valued.
Canadian Occupational Performance MeasureBaseline, 6 months, 13 months.Semi-structured interview including 5 step process to identify subjects' goals. Subjects rate their perceived performance and satisfaction on 1 - 5 goals.

Countries

United States

Contacts

CONTACTSusan Magasi, PhD
smagas1@uic.edu312-996-4603
PRINCIPAL_INVESTIGATORSusan Magasi, PhD

University of Illinois at Chicago

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 22, 2026